Exploiting Live Imaging to Track Nuclei During Myoblast Differentiation and Fusion

Summary

Skeletal muscle differentiation is a highly dynamic process, which particularly relies on nuclear positioning. Here, we describe a method to track nuclei movements by live cell imaging during myoblast differentiation and myotube formation and to perform a quantitative characterization of nuclei dynamics by extracting information from automatic tracking.

Abstract

Nuclear positioning within cells is important for multiple cellular processes in development and regeneration. The most intriguing example of nuclear positioning occurs during skeletal muscle differentiation. Muscle fibers (myofibers) are multinucleated cells formed by the fusion of muscle precursor cells (myoblasts) derived from muscle stem cells (satellite cells) that undergo proliferation and differentiation. Correct nuclear positioning within myofibers is required for the proper muscle regeneration and function. The common procedure to assess myoblast differentiation and myofiber formation relies on fixed cells analyzed by immunofluorescence, which impedes the study of nuclear movement and cell behavior over time. Here, we describe a method for the analysis of myoblast differentiation and myofiber formation by live cell imaging. We provide a software for automated nuclear tracking to obtain a high-throughput quantitative characterization of nuclear dynamics and myoblast behavior (i.e., the trajectory) during differentiation and fusion.

Introduction

Skeletal muscle is the largest tissue in the human body, totaling 35%-40% of body mass¹. Satellite cells are muscle stem cells, anatomically characterized by their position (juxtaposed to the plasma membrane, underneath the basal lamina of muscle fibers), that give rise to proliferating myoblasts (myogenic progenitor cells), which eventually differentiate and integrate into existing myofibers and/or fuse to form new myofibers^2,3,4. Their discovery and the progress in the study of their biology has led to significant insights into muscle development and regeneration.

Protocols to isolate and differentiate myoblasts into myotubes have been developed many years ago and are still widely used to study skeletal muscle differentiation^5,6,7. However, most of these methods represent static procedures that rely on the analysis of fixed cells and, consequently, do not allow scientists to fully explore highly dynamic processes, such as myoblast fusion and myofiber maturation. The most striking example is nuclear positioning, which is tightly regulated, with nuclei initially in the center of the myofiber and, then, located at the periphery after myofiber maturation^8,9. Live imaging is the most appropriate technique to obtain further insights into such a peculiar phenomenon.

Here, we describe a method that enables scientists to record myoblast differentiation and myotube formation by time-lapse microscopy and to perform quantitative analyses from the automatic tracking of myoblast nuclei. This method provides a high-throughput quantitative characterization of nuclear dynamics and myoblast behavior during differentiation and fusion. The protocol is divided into four different parts, namely (1) the collection of muscles from the hindlimbs of mice, (2) the isolation of primary myoblasts that consists in mechanical and enzymatic digestion, (3) myoblast proliferation and differentiation, and (4) live imaging to track nuclei within the first 16 h of myoblast differentiation.

In the following procedure, myoblasts are isolated from H2B-GFP mice and treated with 1 µg/mL of doxycycline to induce H2B-GFP expression, as previously described¹⁰. Alternatively, it is possible to isolate the myoblasts from other transgenic mice that express a fluorescent protein in the nucleus or to transfect the cells isolated from wild-type mice to express a fluorescent protein in the nucleus, as described by Pimentel et al.⁹.

Protocol

All procedures involving animal subjects were approved by the San Raffaele Institutional Animal Care and Use Committee.

1. Dissection of mouse hindlimb muscles

1. Sterilize tweezers and scissors (both straight and curved) by autoclaving.
2. Prepare and filter (0.22 µm) all the media (blocking medium, digestion medium, proliferating medium, and differentiating medium) before starting the experiment (see Table of Materials).
3. Put 5 mL of phosphate-buffered saline (PBS) in a 35 mm Petri dish for muscle collection.
4. Sacrifice the mouse by cervical dislocation or by using CO₂ and sterilize the skin with ethanol. Remove the skin from the hindlimbs and upper limbs by using scissors and tweezers, to facilitate the isolation of muscles.
   NOTE: Muscles can be isolated from neonatal or adult mice. Neonatal mice have an increased number of satellite cells compared to adult mice. However, the total number of satellite cells that can be isolated from a single adult mouse is sufficient to perform the experiment described below.
5. Isolate tibialis, soleus, extensor digitorum longus (EDL), gastrocnemius, quadriceps, and triceps, and put them in the Petri dish containing PBS. Leave the dish on ice. Carefully remove tendons and fat with sterilized scissors and tweezers.

2. Isolation of primary myoblasts

NOTE: All the procedures for cell culture are done in sterile conditions.

1. Remove the muscles from the PBS. Cut and mince the muscles, by using sterile curved scissors, until a uniform mass is obtained. Put the muscle pieces into a 50 mL tube.
2. Add 10 mL of the digestion medium to the muscle pieces and incubate at 37 °C for 30 min under strong agitation (250 min^-1) in a water bath, to enzymatically digest the muscles.
3. Add 10 mL of Dulbecco’s modified Eagle’s medium (DMEM) containing 10% fetal bovine serum (FBS), 1% glutamine, 1% penicillin/streptomycin, and 1% gentamicin (blocking medium) to stop the digestion.
4. Centrifuge at 40 x g for 5 min and collect the supernatant in a 50 mL tube. Save the pellet on ice.
   NOTE: After the centrifugation, the supernatant contains some satellite cells, blood cells, endothelial cells, and fibroblasts, while the pellet contains pieces of undigested muscle and connective tissue. To increase the number of isolated cells, the pellet must be subjected to additional steps of digestion as described below.
5. Centrifuge the supernatant at 650 x g for 5 min. Discard the supernatant and resuspend the pellet in 1 mL of DMEM containing 10% FBS. Keep the resuspended pellet on ice.
6. Repeat steps 2.2–2.5 2x for the rest of the pellet obtained in step 2.4 and add the subsequently resuspended pellets to the first resuspended pellet conserved on ice.
7. Pass the resuspended pellets through a 70 µm filter and then through a 40 µm filter. Add 15 mL of DMEM with 10% FBS, and centrifuge at 650 x g for 5 min.
8. Resuspend the cell pellet in 3 mL of red blood cell lysis buffer to deplete the red blood cells. Incubate it for 5 min at room temperature. Add 40 mL of PBS to stop the lysis of the red blood cells, and centrifuge at 650 x g for 5 min. Remove the supernatant and resuspend the pellet in 5 mL of DMEM with 10% FBS.
9. As preplating step, plate the cells in 20 mL of proliferation medium in a 150 mm uncoated Petri dish. After 1 h of incubation in a cell culture incubator (37 °C, 5% CO₂), collect the medium.
   NOTE: Fibroblasts, attaching to the plate, are then discarded, while satellite cells remain in suspension.
10. Repeat step 2.9 3x and, at the last preplating step, collect the medium which contains the satellite cells in suspension.
11. Centrifuge at 650 x g for 5 min.
12. While the cells are centrifuging, coat two 150 mm Petri dishes with collagen (10 mL of a 0.1% solution in 0.1 M acetic acid). To do so, put the collagen on the plate, incubate for 5 min, and remove it. Let the plate dry for 30 min.
13. Discard the supernatant obtained in step 2.11 and resuspend the cell pellet in 40 mL of proliferation medium (Table of Materials). Plate the cells on two collagen-coated 150 mm Petri dishes (20 mL per dish) and keep the cells in a cell culture incubator (37 °C, 5% CO_2, 5% O₂) in proliferation medium for 2–3 days with 1 µg/mL of doxycycline to induce H2B-GFP expression.
    NOTE: This step allows the proliferation of myoblasts to obtain a higher number of cells for further assays. Cell density is maintained very low to avoid a spontaneous differentiation of myoblasts into myotubes.

3. Myoblast proliferation and differentiation assays

NOTE: When myoblast density is high, some cells initiate elongation, and then, it is necessary to split the cells. Generally, it is possible to split cells 2x–3x without affecting their phenotype.

1. Discard the medium, wash the cells with 5 mL of PBS, add 2 mL of trypsin (1x), and incubate the plate at 37 °C in a cell incubator for 5 min. Check under the microscope and, when round cells detach, add 5 mL of DMEM with 10% FBS to inactivate the trypsin. Count the number of cells (usually it is possible to obtain about 1 x 10⁶ cells/mouse).
   NOTE: Incubation with trypsin for 5 min is usually enough to detach the proliferating myoblasts.
2. Subject the cells to one of the assays described below.
   1. Proliferation assay
      1. Plate 50,000 cells/well in 1 mL/well of proliferation medium in a collagen-coated 12-well plate and incubate the plated cells in a cell culture incubator (37 °C, 5% CO₂). Fix and count the cells at 24, 48, or 72 h.
         NOTE: The medium is replaced every 48 h to avoid nutrient exhaustion.
   2. Differentiation assay
      1. Coat a 12-well plate with 350 µL of differentiation medium containing basement membrane matrix (1:100). Incubate the plate at 37 °C for 30 min and remove the medium.
      2. Plate 200,000 cells/well in the differentiation medium in the matrix-coated plate. Incubate the cells in a cell culture incubator (37 °C, 5% CO_2, 5% O₂) until they adhere to the plate (2 h are generally enough for the cells to adhere and to start differentiation).
      3. To assess differentiation, perform staining for myosin heavy chain and nuclei as previously described¹¹. Alternatively, perform live-imaging analyses as described below.

4. Live-imaging of myoblast differentiation and nuclear tracking

1. For live cell imaging, put the cells, obtained in section 3.2.2 and plated in a 12-well plate, under a confocal microscope, equipped with an incubation system to maintain the cells at 37 °C in 5% CO₂.
2. Use a 20x dry objective (0.7 NA) to get fields of view with hundreds of cells, enough to monitor myofiber formation. H2B-GFP cells can be imaged with a low-intensity 488 nm Argon laser.
   NOTE: An open pinhole ensures that the image depth (~10 µm) contains the cell thickness so that cells are kept in focus throughout the experiment. Using a confocal microscope is advantageous since it improves the signal-to-noise ratio of the images, although wide-field microscopy could also be used. Myofiber formation can be monitored through the transmission channel.
3. Acquire images of 16-bit and 1,024 x 1,024 pixels per frame every 6 min for 16 h. For each acquired position, generate a multiframe.tif file (see example in the Supplementary Files).
   NOTE: In the present protocol, commercial software associated with the microscope (Table of Materials) has been used; use the appropriate software to achieve the same goal when using other microscopes.
4. Download the software provided as a .zip supplementary file.
   NOTE: The routines are scripts that must be run in MATLAB. The software is an adaptation of a published software¹² optimized for the tracking of the nuclei during myotube formation. This software is divided into two parts: the first one identifies the nuclei in each frame by segmenting them, while the second one generates “tracks” (trajectories) of nuclei movement. The complete code for nuclear segmentation and tracking and a step-by-step guide to getting started are provided in the Supplementary Files.
5. Extract the zip file and save it in a desired path on the personal computer (PC) in use. Perform all the below passages on a PC with the necessary software already installed. Note that the .zip file is composed of three folders as mentioned below.
   NOTE: Segmentation Routines contains the functions to be run for the segmentation. Tracking Routines, instead, contains the functions required for the tracking. Example Segmentation Tracking provides the basic scripts and files to get acquainted with the system. The software used for segmentation and tracking of the nuclei runs properly in MATLAB, R2015a or later versions.
6. To segment the nuclei from the .tif file, name the file, for example, NameFile.tif.
   1. Open the Example Segmentation Tracking folder and click on DoSegmentation.m. This will open the command window in MATLAB.
   2. Check the Current Folder window on the left to see all the elements in the Example of Segmentation Tracking folder. Double-click on DoSegmentation.m.
      NOTE: Detailed information on the modifications that have to be done in the script can be found in the StepbyStep.txt file. It is mandatory to modify the script so that the variable filenameinput is NameFile.tif and folderinput is the folder where the .tif file is contained.
   3. Run the script (by clicking on the green Run button). The result of the segmentation will be saved as a file.mat (SegmentedNameFile.mat), while the segmentation of the nuclei can be visualized in the output figure.
      NOTE: Parameters for the segmentation, described in the script, can be modified if needed. The quality of the segmentation can be checked using the script CheckSegmentation.m (see the StepbyStep.txt file). Based on this, if the quality of the segmentation is poor (only a few nuclei detected), adjust the parameters of the segmentation, clearly indicated in the DoSegmentation.m script, and repeat the procedure.
7. To generate the tracks (i.e., the trajectories of each of the nuclei in time), using the nuclear positions obtained in the segmentation, run the script GenerateTracks.m in the same working folder. Be sure to add the proper segmentation file as an input, obtained before (see the StepbyStep.txt file for further information).
   NOTE: As an output, the user will obtain a file TrackedNameFile.mat, with a matrix for the x-coordinates and another matrix for the y-coordinates of the generated tracks.
8. Evaluate the quality of the tracks using CheckTracking.m (see the StepbyStep.txt file for further information). Use the output figure of this last passage to help visualize each nuclei position in time. Check on the left for green crosses that indicate each segmented nucleus. To select one specific nucleus, use the lower scrollbar. Note that the selected nucleus will be circled in red, while on the right, the trajectory of the selected cell can be followed in time (by using the upper scrollbar).

Results

To automatically follow nuclear movement during myoblast differentiation in live imaging, the nuclei should preferentially be fluorescently labeled. It is important to note that using DNA-intercalating molecules is not feasible because these molecules interfere with the proliferation and differentiation of primary myoblasts¹³. As an example, proliferation and differentiation have been analyzed in primary myoblasts cultured with or without Hoechst (

Discussion

Muscle fibers (myofibers) are multinucleated cells that are formed by the fusion of muscle precursors cells (myoblasts) derived from muscle stem cells (satellite cells) that undergo proliferation and differentiation^2,3,4. To assess myoblast differentiation, the common procedure consists of culturing myoblasts in differentiating medium and fixing the cells at different time points to perform immunofluorescence staining for MyHC, ...

Materials

Name	Company	Catalog Number	Comments
chicken embryos extract	Seralab	CE-650-J
collagenase	Sigma	C9263-1G	125units/mg
collagen from calf skin	Sigma	C8919
dispase	Gibco	17105-041	1.78 units/mg
doxyciclin	Sigma	D1515
DMEM	Sigma	D5671
fetal bovine serum	Life technologies	10270106
gentamicin	Sigma	G1397
Horse serum	Invitrogen	16050-098
Hoechst	life technologies	33342
IMDM	Sigma	I3390
L-glutamine	Sigma	G7513
Matrigel	Corning	356231
penicillin-streptomycin	Sigma	P0781
red blood cells lysis medium	Biolegend	420301
Digestion medium
collagenase	40 mg
dispase	70 mg
PBS	20 ml
filtered 0.22um
Blocking medium
DMEM
Fetal bovine serum	10%
L-glutammine	1%
penicillin-streptomycin	1%
gentamicin	1 ‰
filtered 0.22um
proliferation medium
IMDM
Fetal bovine serum	20%
L-glutammine	1%
penicillin-streptomycin	1%
gentamicin	1 ‰
chichen embryo extract	3%
filtered 0.22um
differentiation medium
IMDM
Horse serum	2%
L-glutammine	1%
penicillin-streptomycin	1%
gentamicin	1 ‰
chichen embryo extract	1%
filtered 0.22um